iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs13459245	snp	A/G	0.375	0.216506	missense, upstream-variant-2KB	Nck1	GRCm38.p3	9:100508644	GAAAGATGGCTGAAG[A/G]AGTGGTGGTGGTGGC	17973
rs29597018	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Nck1	Mm_Celera	9:100508772	GAGGCCAGGAATTAT[A/G]ACTCATACCAGCAAA	17973
rs29645256	snp	A/G/T	0.444444	0.157135	intron-variant	Nck1	GRCm38.p3	9:100519995	AAAAAAAGAAAGAAA[A/G/T]AACTACCTTCAAAAA	17973
rs29649401	snp	C/G	0.387812	0.208586	intron-variant	Nck1	Mm_Celera	9:100533088	ACACATCCTTTTACA[C/G]AAACAAACAAACCAC	17973
rs29686533	snp	A/C	0.46875	0.121031	intron-variant	Nck1	Mm_Celera	9:100521523	ATGCCTGTCTCTTTG[A/C]CTGGCTTGTATTTTA	17973
rs29688436	snp	C/T	0.375	0.216506	intron-variant	Nck1	Mm_Celera	9:100522454	TAAGCCACAACATCA[C/T]ATAGTTTATATTGCT	17973
rs29689723	snp	C/T	0.484429	0.0868505	intron-variant	Nck1	GRCm38.p3	9:100506437	GCTTTACTTCAAATG[C/T]CTGTGTGTGGTACAA	17973
rs29691374	snp	C/T	0.487535	0.077957	intron-variant	Nck1	GRCm38.p3	9:100509231	TTCTGAACACTTTTG[C/T]CTTCCCATATAAGTT	17973
rs29694935	snp	G/T	0.48	0.0979796	intron-variant	Nck1	Mm_Celera	9:100500797	TTTTTTTTTTTTTTT[G/T]TACTGAGTTTTTTGT	17973
rs29696025	snp	A/T	0.48	0.0979796	intron-variant	Nck1	Mm_Celera	9:100542905	GATCACATTAGAACA[A/T]AATTTGAGCAACAAT	17973
rs29740236	snp	A/C	0.375	0.216506	intron-variant	Nck1	Mm_Celera	9:100538245	GAACCTAGAGTTACA[A/C]AGCTCCATTGCAGAA	17973
rs29745633	snp	G/T	0.487535	0.077957	intron-variant	Nck1	Mm_Celera	9:100498597	CAATGTCTTATACTC[G/T]ATTACTTGTCTGCTT	17973
rs29748244	snp	C/T	0.473373	0.11227	upstream-variant-2KB	Nck1	Mm_Celera	9:100547788	TAAAGGAAATAAGAA[C/T]CCTCCATATCTTAAG	17973
rs29787950	snp	C/T	0.444444	0.157135	intron-variant	Nck1	Mm_Celera	9:100511194	TATAAGGTAGAGAGC[C/T]ATTAAAGAAGGCATG	17973
rs29790474	snp	C/T	0.375	0.216506	intron-variant	Nck1	Mm_Celera	9:100541264	AATTTCTGCCTCTCC[C/T]AAGGAAATGTTTCCA	17973
rs29791574	snp	A/G	0.444444	0.157135	intron-variant	Nck1	Mm_Celera	9:100496834	AGACCGAGTTATACA[A/G]TGAGTCATTCTCTCA	17973
rs29793198	snp	G/T	0.387812	0.208586	intron-variant	Nck1	Mm_Celera	9:100526153	CGTGTGTGAATGCTT[G/T]TGGTACCATTCAGCT	17973
rs29839551	snp	A/G	0.444444	0.157135	intron-variant	Nck1	Mm_Celera	9:100540397	ATACATCATGGAAAA[A/G]AGACATGCAGTAAAA	17973
rs29840671	snp	A/C/T	0.444444	0.157135	intron-variant	Nck1	GRCm38.p3	9:100496590	AGAATTTTTAAAAAA[A/C/T]AACTGTCAAATTTTA	17973
rs29841207	snp	A/G	0.455	0.143091	intron-variant	Nck1	Mm_Celera	9:100495946	AAAGTAGTGAACACA[A/G]AAAGTAGTTTTCAGA	17973
rs29921954	snp	C/T	0.498615	0.0262793	intron-variant	Nck1	Mm_Celera	9:100506616	ACCAGCTTACATAAA[C/T]CCACTGAGTTCTTTC	17973
rs29931030	snp	A/T	0.48	0.0979796	upstream-variant-2KB	Nck1	Mm_Celera	9:100547821	CTTTCCCAGTAAGCT[A/T]TTGACAGCTTATATA	17973
rs29932990	snp	A/G	0.46875	0.121031	intron-variant	Nck1	Mm_Celera	9:100525564	TTCAGCTCATTCTGC[A/G]GGCAGTGACTACCTG	17973
rs29940234	snp	C/T	0.48	0.0979796	intron-variant	Nck1	Mm_Celera	9:100545082	TTTCTCCTTGGACTA[C/T]TTCTCTGTTCATGTT	17973
rs29974548	snp	A/G	0.375	0.216506	intron-variant, utr-variant-3-prime	Nck1	Mm_Celera	9:100494989	TGGCTTGTGACAGAT[A/G]CAATATCTGAAAATA	17973
rs29982802	snp	C/T	0.48	0.0979796	intron-variant	Nck1	Mm_Celera	9:100527074	TGCTATCCTACATTT[C/T]TTAGAAATGCATAAA	17973
rs30040183	snp	C/T	0.475309	0.108333	intron-variant	Nck1	Mm_Celera	9:100523422	CAAACTGTGAAAATG[C/T]ATAACAAAGAATTGC	17973
rs30041229	snp	A/G	0.375	0.216506	intron-variant	Nck1	GRCm38.p3	9:100539186	GAACAGAGGCAGGCC[A/G]ATCCCTGGGATTTCA	17973
rs30086437	snp	C/T	0.48	0.0979796	intron-variant	Nck1	Mm_Celera	9:100543305	CATCACAAAACACAC[C/T]GCTCTGTGCGCTAAC	17973
rs30176812	snp	C/T	0.5	0	intron-variant	Nck1	Mm_Celera	9:100530167	GCAGATAAATAAAGG[C/T]ACTTGTCACACAAGC	17973
rs30182162	snp	C/T	0.375	0.216506	intron-variant	Nck1	Mm_Celera	9:100505139	CAGTGAGTTCTAAGA[C/T]ATCCAGGAACACACT	17973
rs30183511	snp	C/T	0.5	0	downstream-variant-500B	Nck1	Mm_Celera	9:100494484	CTCAGCGCAGAACAC[C/T]TGCTTTTCATGTGTA	17973
rs30231492	snp	G/T	0.444444	0.157135	intron-variant	Nck1	Mm_Celera	9:100540794	TCTGTTTTGGCTAGG[G/T]TTTTGCTGCTGTTTT	17973
rs30233201	snp	A/G	0.444444	0.157135	intron-variant	Nck1	Mm_Celera	9:100542264	AACACACACAAAAAA[A/G]GGGAGGATAGGCAAA	17973
rs30276774	snp	C/G	0.375	0.216506	intron-variant	Nck1	Mm_Celera	9:100538459	GTTACATATAACAAA[C/G]CCACAGCCAGTATCA	17973
rs30327786	snp	A/G	0.5	0	intron-variant, utr-variant-5-prime	Nck1	Mm_Celera	9:100545979	GTGTGTCCGCACGCG[A/G]GCGAGGCCGTCTCAC	17973
rs30334000	snp	A/T	0.465374	0.126941	intron-variant	Nck1	Mm_Celera	9:100526518	AGGCAGCAAACTTCT[A/T]AGGTGAACAAACAAG	17973
rs30373936	snp	C/T	0.5	0	intron-variant	Nck1	Mm_Celera	9:100537065	ATATCATCATTGCTA[C/T]TATTATTATATTATT	17973
rs30384351	snp	C/T	0.375	0.216506	intron-variant	Nck1	Mm_Celera	9:100532356	TTACATAAAATAAAT[C/T]CCAGCATGCATATAT	17973
rs30386257	snp	A/G/T	0.387812	0.208586	intron-variant	Nck1	GRCm38.p3	9:100535064	CTTGGGTTCTGCACT[A/G/T]AGATGACAAAGCAAG	17973
rs30387273	snp	A/G	0.444444	0.157135	intron-variant	Nck1	Mm_Celera	9:100538157	AAGAACTAGCAAAGA[A/G]CAAAACAAACTCAAC	17973
rs30427730	snp	A/G	0.5	0	intron-variant	Nck1	GRCm38.p3	9:100514509	CTCACACAGACATAT[A/G]TGCAAGTAACACCAA	17973
rs30430419	snp	C/T	0.5	0	intron-variant	Nck1	Mm_Celera	9:100544601	CTGGCATTGAAAGCA[C/T]CCATTCTTCCACATT	17973
rs30438113	snp	G/T	0.375	0.216506	intron-variant	Nck1	Mm_Celera	9:100532450	CAGATGATGATGATG[G/T]TGGATCCTCGGAATC	17973
rs30438859	snp	A/T	0.5	0	intron-variant	Nck1	Mm_Celera	9:100510546	ATTGACTACCATGTC[A/T]GTTTTCTCAACAATG	17973
rs30478816	snp	C/T	0.48	0.0979796	intron-variant	Nck1	Mm_Celera	9:100520416	GCTTTCTGTCTCTGT[C/T]TCCCAAGTGCTGGGA	17973
rs30486532	snp	C/T	0.498615	0.0262793	intron-variant	Nck1	Mm_Celera	9:100499034	TCCTTAATTTCCTTA[C/T]TTCTGGCTAATGAGG	17973
rs30516612	snp	C/T	0.456747	0.140554	intron-variant	Nck1	Mm_Celera	9:100525987	ACATCAGAATTGACT[C/T]AGATGTTCACGGGTC	17973
rs33198484	snp	C/T	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100502163	TCACCTAACCATTTA[C/T]GTGATAATTACCAAG	17973
rs33198485	snp	C/T	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100502725	TCTAGCATTTTAGTT[C/T]ACCACAATCATCCTA	17973
rs33198486	snp	G/T	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100502752	CCTACCTTCAATTTG[G/T]TTTTTTTTCCCCAAA	17973
rs33198487	snp	C/T	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100502790	ATTCCATTGCTACTC[C/T]TATTCTGATTGTAAG	17973
rs33198488	snp	G/T	0.5	0	intron-variant	Nck1	Mm_Celera	9:100502799	CTACTCTTATTCTGA[G/T]TGTAAGTCTTAAGGG	17973
rs33198489	snp	C/T	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100502820	GTCTTAAGGGGTCTA[C/T]TATGAAAACTTAAAA	17973
rs33198490	snp	G/T	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100503035	GATAACAGTTGTCAG[G/T]TTTTTTTTGTTATTT	17973
rs33198491	snp	A/T	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100503147	ACACTGAGGAGGGAG[A/T]TAACTCTGAAGCAGT	17973
rs33198492	snp	G/T	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100504008	GATAGTGTTATTCTT[G/T]CTCAGGCAAATCTTT	17973
rs33198493	snp	A/C	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100504104	GAAAGCATCAGATAC[A/C]AAGTGAACAAACTGC	17973
rs33198524	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100528797	AGGAAGTTGTTGTTG[A/G]CCAGTGACAGACCTG	17973
rs33198525	snp	A/C	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100531102	GTAATTTCTTTTTCT[A/C]AGTTTTAATGATATG	17973
rs33198526	snp	A/G	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100531420	TTTGGATTCATAAGA[A/G]AAGCATCTCTTCTCT	17973
rs33198527	snp	A/T	0.277778	0.248452	intron-variant	Nck1	Mm_Celera	9:100531712	GATACATTTTAAACT[A/T]TTTAAACTATAAGTT	17973
rs33198528	snp	C/T	0.18	0.24	intron-variant	Nck1	Mm_Celera	9:100531713	ATACATTTTAAACTA[C/T]TTAAACTATAAGTTT	17973
rs33198529	snp	C/T	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100531938	CACTGTGTGACCCTG[C/T]GCATCACAGCACCCG	17973
rs33198530	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100532021	GCTTCTAGCCTAGAT[A/G]AGAAAGCACAAGCCC	17973
rs33198531	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100532708	TGAAATAATAACAAA[A/G]TGAGCATCTACATCT	17973
rs33198532	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100532820	TCAGGACTCATGTAA[A/G]TATCTTCTATTAAAC	17973
rs33198533	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100532851	TCCCAAAGAGTTCCA[A/G]AAAGTATAATAAAAT	17973
rs33199294	snp	A/G	0.497778	0.0332592	intron-variant	Nck1	Mm_Celera	9:100504123	TGAACAAACTGCCAC[A/G]TTTAGCTGGCCAGAA	17973
rs33199295	snp	A/G	0.244898	0.249948	intron-variant	Nck1	Mm_Celera	9:100504218	ATGGAGTTCTGCACC[A/G]ACACAACCACAGCAG	17973
rs33199296	snp	G/T	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100504249	CTCTTACTAAATTTT[G/T]TTCTTTGTGTCAGCC	17973
rs33199297	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100504359	ACTAAGTAAATGCTC[A/G]ACAGAATGGGTTCAG	17973
rs33199298	snp	G/T	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100504522	TGTAGAGCTGGAAGG[G/T]ACTTTCCAGGATCAT	17973
rs33199299	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100504851	ATTTAGAAGTTAGGT[A/G]AATGAAAACCTGTCT	17973
rs33199300	snp	A/G	0.260355	0.249785	intron-variant	Nck1	Mm_Celera	9:100504901	AGCAAAATAAACATC[A/G]ATATTATAGGGATTG	17973
rs33199301	snp	A/G	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100504982	ACAGATACAGTTAGG[A/G]CTGAATATGCTTTAT	17973
rs33199302	snp	A/G	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100505270	TCATCTAACTCCCTA[A/G]CAGATTCTGCAAGAG	17973
rs33199303	snp	C/T	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100505486	TGCTGAACAATCTTG[C/T]CAAACCATCGAGCTG	17973
rs33199474	snp	C/T	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100533168	TTAAAGGAATATATG[C/T]ACACAAGCCAGGGCA	17973
rs33199475	snp	C/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100533226	ATACACTTGTATTTA[C/G]TTCATATCCATCAAG	17973
rs33199476	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100533296	CTACCTATTCTGATG[A/G]CTAGTACTGTATACT	17973
rs33199477	snp	A/G	0.132653	0.220748	intron-variant	Nck1	Mm_Celera	9:100533299	CCTATTCTGATGGCT[A/G]GTACTGTATACTACT	17973
rs33199478	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100533330	AGCTCTTCCCATTGA[A/G]TGCACTTCTCTGACC	17973
rs33199479	snp	A/C	0.391111	0.206368	intron-variant	Nck1	Mm_Celera	9:100533367	TCTACAACTTTAGCT[A/C]TCTCAGTAGACACAA	17973
rs33199480	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100533375	TTTAGCTATCTCAGT[A/G]GACACAACTACAGAC	17973
rs33199481	snp	A/G	0.408163	0.193609	intron-variant	Nck1	Mm_Celera	9:100533524	AACAAGCTTCGTGAT[A/G]CGAGGGTAGGGTCAG	17973
rs33199482	snp	A/G	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100533740	TCTTATAGATGTTGG[A/G]GAAAATACAAGGATG	17973
rs33199483	snp	A/T	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100533878	CTCTAAACTCAACAT[A/T]TAAGAGTCCAGCAAG	17973
rs33200064	snp	A/C	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100505904	CTCAAAGATCTAAAA[A/C]TGTATTTGTTCTCTA	17973
rs33200065	snp	C/T	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100506065	CTCTTGGACTCTCAT[C/T]AGATCACTGTTTCCT	17973
rs33200066	snp	C/T	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100506089	GTTTCCTTAGGCTTT[C/T]TGACTCTTAAGAGAC	17973
rs33200067	snp	A/G	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100506243	TTTACTTGTAAGTCA[A/G]TACTTGTAGTTTACT	17973
rs33200068	snp	A/G	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100506262	TTGTAGTTTACTAGA[A/G]CTCTTATTAAATGTT	17973
rs33200069	snp	C/T	0.32	0.24	intron-variant	Nck1	Mm_Celera	9:100506292	TATCTTGACATTATT[C/T]CAACAAAGCTTAAGT	17973
rs33200070	snp	C/T	0.231111	0.249285	intron-variant	Nck1	Mm_Celera	9:100506564	GCAGTGAAAATATCA[C/T]CGCCATTTACCTTCT	17973
rs33200071	snp	A/G	0.142012	0.225474	intron-variant, utr-variant-5-prime	Nck1	Mm_Celera	9:100506992	CAAGTAACTCAGGGC[A/G]GCAGCAAAAACAGGA	17973
rs33200072	snp	A/T	0.244898	0.249948	intron-variant, utr-variant-5-prime	Nck1	Mm_Celera	9:100507036	CATTGTAACAGAAAA[A/T]ATTAAAGCTAGTATG	17973
rs33200073	snp	G/T	0.277778	0.248452	intron-variant, upstream-variant-2KB	Nck1	Mm_Celera	9:100507522	AAGAAACATTTACCT[G/T]ATATTGCCAATAATT	17973
rs33200174	snp	C/T	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100534356	GCTGTAAGAACCACT[C/T]TGTGTCAGCTCCTGA	17973
rs33200175	snp	A/G	0.124444	0.216185	intron-variant	Nck1	Mm_Celera	9:100534405	CTGCTGTCCTTGCAG[A/G]TCCTCTATAGTCTGT	17973

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